Hormones and Cancer by Herbert W. Dickerman, S. Anand Kumar (auth.), Wendell W.

By Herbert W. Dickerman, S. Anand Kumar (auth.), Wendell W. Leavitt (eds.)

The papers during this quantity have been provided on the Symposium on Hormones and melanoma held March 24-26, 1980, on the Worcester origin for Experimental Biology, Shrewsbury, MA. The assembly was once equipped to check fresh advances in uncomplicated and scientific learn paintings on hormone-responsive tumors of the reproductive approach. The organization among protracted hormone motion and melanoma of the reproductive method is now irrefutable. but we nonetheless have no idea how hormones begin and advertise neoplastic transformation in their objective cells. a tremendous attempt is cur­ rently being directed at realizing the hormonal rules of neoplastic cells, specifically these coming up from the breast, uterus, pituitary gland and prostate. The symposium introduced jointly best specialists whose learn is concentrated in this impor­ tant region of human overall healthiness. even if many questions stay to be responded via destiny stories, the fabric lined during this quantity presents an updated evaluation of the present prestige of labor during this sector. the themes variety from the mechanism of hormone motion to the remedy of hormone-dependent tumors, and subject matters comprise estrogen, progestin, androgen and glucocorticoid motion~ hormone receptors~ particular protein responses~ developmental results of estrogens and antiestrogens~ the DES syndrome~ regu­ lation of the cellphone cycle~ healing results of antiestrogens, aromatase inhibitors, iodoestrogens, progestins on estrogen­ established tumors~ characterization of retinoid-binding websites~ and the software of assorted tumor markers.

Show description

Read Online or Download Hormones and Cancer PDF

Similar cancer books

Therapeutic Resistance to Anti-hormonal Drugs in Breast Cancer: New Molecular Aspects and their Potential as Targets

One of many major motives of failure within the therapy of breast melanoma is the intrinsic presence of, or improvement of, drug resistance by way of the melanoma cells. contemporary reviews at the mechanisms of melanoma drug resistance have yielded vital info highlighting either how tumour cells may well get away those healing constraints and that drug resistance may well extra impinge on tumour cellphone services which can eventually advertise an adversarial phone phenotype.

An Omics Perspective on Cancer Research

Omics is an rising and intriguing quarter within the box of technology and medication. a number of promising advancements were elucidated utilizing omics (including genomics, transcriptomics, epigenomics, proteomics, metabolomics, interactomics, cytomics and bioinformatics) in melanoma learn. the improvement of high-throughput applied sciences that allow the answer of decoding melanoma from better dimensionality will offer a data base which alterations the face of melanoma figuring out and therapeutics.

Cancer Active Immunotherapy: Immunoprophylaxis and Immunorestoration

I want to thank all my co-workers who've collaborated with me, from 1963 formerly, in organic and scientific learn within the box of melanoma lively immunotherapy, of its immuno­ prevention and immunorestoration. they are going to frequently be quoted during this publication. i'm fairly thankful to people who have helped me to jot down it by means of reviewing a few chapters: D.

Extra resources for Hormones and Cancer

Example text

S. R. (1978) Biochem. J. 170, 331-335. S. D. (1978) J. BioI. Chern. 253, 3494-3503. Y. & Capony, F. (1979) J. Steroid Biochem. 11, 231-236. Lazier, c:B. J. (1979) Biochem. J. 180, 347-353. Gschwendt, M. (1977) Eur. J. Biochem. -Gschwendt, M. & Kittstein, W. (1974) Biochim. Biophys. Acta 361, 84-96. , Mester, J. -E. , Fromageot, P. , eds),North Holland Publishers, Amsterdam, pp. 183-195. , Tran, A. -E. (1979) Nucleic Acids Res. 7, 2031-2044. F. S. W. , eds), Plenum Press, New York, pp. 47-70. Gschwendt, M.

Chern. 358, 1583-1590. , Eriksson, H. W. W. , eds), Plenum Press, New York, pp. 17-46. , Binastein, M. F. (1977) J. BioI. Chern. 252, 8310-8319. , Panyim, S. P. (1978) Eur. J. Biochem. 84, 355-364. , Milius, R. & Alaupovic, P. (1980) Compo Biochem. Physiol. 65B, 231-237. R. E. L. , eds), Academic Press, London, in press. , Mester, J. -E. (1977) Nature 267, 434-435. B. S. (1977) Biochem. J. 164, 659-667. , Capony, F. L. L. , eds), Academic Press, London, in press. -L. L. (1980) manuscript submitted.

Proposed Pathway of DES Metabolism in the past to be responsible for its formation (10,38). It should be evident from Fig. 1 and the above-mentioned text that the hormonal, toxic and/or fetotoxic nature of DES may reside in one or a number of the above-mentioned compounds. Considering the extensive metabolism of DES, it is interesting to determine whether the established hormonal activity resides in the parent compound or one of the various metabolites. Estrogenicity of these compounds was analyzed in the mouse uterus because of the marked sensitivity of this tissue to estrogens (39) and because of its possible correlation with previous studies involving metabolism (19) and toxicity (7) of DES in the mouse.

Download PDF sample

Rated 4.84 of 5 – based on 26 votes